Site Activation Coordinator

hace 4 semanas


Ciudad de México IQVIA A tiempo completo

Job OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions- Under general supervision, perform site activation activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions, working closely with the Site Activation Manager (SAM), Project Management team, and other departments as necessary. Review documents for completeness, consistency and accuracy, under guidance of senior staff.- Prepare site regulatory documents, reviewing for completeness and accuracy.- Inform team members of completion of regulatory and contractual documents for individual sites.- Distribute completed documents to sites and internal project team members.- Support the updating and maintenance of internal systems, databases, tracking tools, timelines and project plans with accurate and complete project specific information.- Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF) and Investigator Pack (IP) release documents.**Qualifications**:- Bachelor's Degree Life sciences or a related field.- 1 years’ experience in a healthcare environment or equivalent combination of education, training and experience. Productive individual contributor who works under general supervision. Problems faced are generally routine but may require interpreting proceedures or policies to resolve.- Good interpersonal communication and organizational skills.- Good attention to detail.- General awareness clinical trial environment and drug development process.- Ability to work on multiple projects.- Ability to establish and maintain effective working relationships with co-workers, managers and sponsors.



  • Ciudad de México IQVIA A tiempo completo

    Job OverviewUnder general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential Functions- Under general...


  • Ciudad de México IQVIA A tiempo completo

    **Job Overview** Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. **Essential Functions** - Under...


  • Ciudad de México IQVIA A tiempo completo

    Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions - Under general...


  • Ciudad de México, CDMX IQVIA A tiempo completo

    Job Overview Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions - Under general...


  • Ciudad de México IQVIA A tiempo completo

    **Job Overview**Under general supervision, perform tasks at a country level associated with site activation activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.**Essential Functions**- Under...


  • Ciudad de México ICON Plc A tiempo completo

    Senior Site Activation LeadICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are currently seeking Senior Site Activation Lead to join our diverse...


  • Ciudad de México, Ciudad de México IQVIA A tiempo completo

    Associate Site Activation Manager – Sponsor Dedicated Direct and manage the delivery of all required site activation, maintenance and regulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work and resources.You will: Oversee the execution of Site Activation and Maintenance for...


  • Ciudad de México Novasyte A tiempo completo

    Job OverviewUnder moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level.Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors; maintains,...


  • Ciudad de México Novasyte A tiempo completo

    Job Overview Under moderate supervision, executes the feasibility, site identification regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional, or country level. Prepares and manages site documentation; reviews and negotiates site documents and contracts with sites and sponsors;...

  • Site Activation Partner

    hace 2 semanas


    Ciudad de México Parexel A tiempo completo

    Parexel is looking for a Site Activation partner in Mexico to join our company!The Site Activation Partner is responsible for leading or supporting operational activities from start-up to close-out, for assigned studies and investigator sites to ensure compliance with study timelines and in accordance with prevailing laws, Good Clinical Practices, and Client...